Rowczenio DM - Search Results

1

Molecular genetic investigation, clinical features, and response to treatment in 21 patients with Schnitzler syndrome.

Rowczenio DM, Pathak S, Arostegui JI, Mensa-Vilaro A, Omoyinmi E, Brogan P, Lipsker D, Scambler T, Owen R, Trojer H, Baginska A, Gillmore JD, Wechalekar AD, Lane T, Williams R, Youngstein T, Hawkins PN, Savic S, Lachmann HJ. Rowczenio DM, et al. Blood. 2018 Mar 1;131(9):974-981. doi: 10.1182/blood-2017-10-810366. Epub 2017 Dec 28. Blood. 2018. PMID: 29284595 Free PMC article. Clinical Trial.

2

Colchicine responsive periodic fever syndrome associated with pyrin I591T.

Fisher BA, Lachmann HJ, Rowczenio D, Goodman HJ, Bhalara S, Hawkins PN. Fisher BA, et al. Ann Rheum Dis. 2005 Sep;64(9):1384-5. doi: 10.1136/ard.2004.030379. Ann Rheum Dis. 2005. PMID: 16100353 Free PMC article. No abstract available.

3

Autosomal dominant periodic fever with AA amyloidosis: tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in a Turkish family.

Dinc A, Erdem H, Rowczenio D, Simsek I, Pay S, Bahce M, Lachmann H. Dinc A, et al. J Nephrol. 2005 Sep-Oct;18(5):626-9. J Nephrol. 2005. PMID: 16299693

4

AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: a report of two cases.

Lachmann HJ, Goodman HJ, Andrews PA, Gallagher H, Marsh J, Breuer S, Rowczenio DM, Bybee A, Hawkins PN. Lachmann HJ, et al. Among authors: rowczenio dm. Arthritis Rheum. 2006 Jun;54(6):2010-4. doi: 10.1002/art.21901. Arthritis Rheum. 2006. PMID: 16732551 Free article.

5

Organ transplantation in hereditary apolipoprotein AI amyloidosis.

Gillmore JD, Stangou AJ, Lachmann HJ, Goodman HJ, Wechalekar AD, Acheson J, Tennent GA, Bybee A, Gilbertson J, Rowczenio D, O'Grady J, Heaton ND, Pepys MB, Hawkins PN. Gillmore JD, et al. Am J Transplant. 2006 Oct;6(10):2342-7. doi: 10.1111/j.1600-6143.2006.01507.x. Epub 2006 Aug 21. Am J Transplant. 2006. PMID: 16925563 Free article.

6

Successful treatment of familial Mediterranean fever with Anakinra and outcome after renal transplantation.

Moser C, Pohl G, Haslinger I, Knapp S, Rowczenio D, Russel T, Lachmann HJ, Lang U, Kovarik J. Moser C, et al. Nephrol Dial Transplant. 2009 Feb;24(2):676-8. doi: 10.1093/ndt/gfn646. Epub 2008 Nov 25. Nephrol Dial Transplant. 2009. PMID: 19033248

7

Diagnosis, pathogenesis, treatment, and prognosis of hereditary fibrinogen A alpha-chain amyloidosis.

Gillmore JD, Lachmann HJ, Rowczenio D, Gilbertson JA, Zeng CH, Liu ZH, Li LS, Wechalekar A, Hawkins PN. Gillmore JD, et al. J Am Soc Nephrol. 2009 Feb;20(2):444-51. doi: 10.1681/ASN.2008060614. Epub 2008 Dec 10. J Am Soc Nephrol. 2009. PMID: 19073821 Free PMC article.

8

An unusual phenotype in Muckle-Wells syndrome associated with NLRP3 E311K.

Murphy G, Daly M, O'Sullivan M, Stack J, Rowczenio D, Lachmann H, Shanahan F, Harney S, Hawkins P, Molloy M. Murphy G, et al. Rheumatology (Oxford). 2011 Feb;50(2):419-20. doi: 10.1093/rheumatology/keq280. Epub 2010 Sep 5. Rheumatology (Oxford). 2011. PMID: 20819795 No abstract available.

9

Outcome in renal Al amyloidosis after chemotherapy.

Pinney JH, Lachmann HJ, Bansi L, Wechalekar AD, Gilbertson JA, Rowczenio D, Sattianayagam PT, Gibbs SD, Orlandi E, Wassef NL, Bradwell AR, Hawkins PN, Gillmore JD. Pinney JH, et al. J Clin Oncol. 2011 Feb 20;29(6):674-81. doi: 10.1200/JCO.2010.30.5235. Epub 2011 Jan 10. J Clin Oncol. 2011. PMID: 21220614

10

Amyloidogenicity and clinical phenotype associated with five novel mutations in apolipoprotein A-I.

Rowczenio D, Dogan A, Theis JD, Vrana JA, Lachmann HJ, Wechalekar AD, Gilbertson JA, Hunt T, Gibbs SD, Sattianayagam PT, Pinney JH, Hawkins PN, Gillmore JD. Rowczenio D, et al. Am J Pathol. 2011 Oct;179(4):1978-87. doi: 10.1016/j.ajpath.2011.06.024. Epub 2011 Aug 5. Am J Pathol. 2011. PMID: 21820994 Free PMC article.

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